Exhibit 16-3
Consider the data below to answer the following question(s).
The −NH₂ group is listed in our textbook as the strongest o,p-directing activator in electrophilic aromatic substitution reactions.However,when aniline is subjected to standard nitration conditions poor yields of m-nitroaniline result.
-Refer to Exhibit 16-3.Draw all the resonance forms of aniline showing the electron-donating effect of the −NH₂ substituent.

Question

Exhibit 16-3
Consider the data below to answer the following question(s).
The −NH₂ group is listed in our textbook as the strongest o,p-directing activator in electrophilic aromatic substitution reactions.However,when aniline is subjected to standard nitration conditions poor yields of m-nitroaniline result.

Exhibit 16-3 Consider the data below to answer the following question(s). The −NH<sub>2</sub> group is listed in our textbook as the strongest o,p-directing activator in electrophilic aromatic substitution reactions.However,when aniline is subjected to standard nitration conditions poor yields of m-nitroaniline result. -Refer to Exhibit 16-3.Draw all the resonance forms of aniline showing the electron-donating effect of the −NH<sub>2</sub> substituent.

-Refer to Exhibit 16-3.Draw all the resonance forms of aniline showing the electron-donating effect of the −NH₂ substituent.

Quizplus · Accepted Answer

The Answer of Exhibit 16-3 Consider the data below to answer the following question(s). The −NH 2 group is listed in our textbook as the strongest o,p-directing activator in electrophilic aromatic substitution reactions.However,when aniline is subjected to standard nitration conditions poor yields of m-nitroaniline result. -Refer to Exhibit 16-3.Draw all the resonance forms of aniline showing the electron-donating effect of the −NH₂ substituent.

Exhibit 16-3 Consider the Data Below to Answer the Following Question(s)